Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2376805
GABRD
1 2024923 non coding transcript exon variant G/A snv 0.80 0.81 1
rs28536160
AVPR1B
1 206117948 intron variant A/G snv 0.19 1
rs3794808
SLC6A4
17 30204775 intron variant C/T snv 0.43 1
rs4131347 12 71930591 downstream gene variant G/A;C snv 1
rs78809014
LOC102723468 ; MAPKAP1
9 125542973 intron variant C/G snv 5.8E-03 2.2E-03 1
rs885861
VIPR2 ; LINC00689
7 159028856 3 prime UTR variant G/A snv 0.43 1
rs10868235
NTRK2
0.925 0.040 9 84878840 intron variant C/T snv 0.40 6
rs4630333
TIMELESS
0.882 0.040 12 56443632 intron variant C/T snv 0.33 4
rs6774721 1.000 0.040 3 49344465 upstream gene variant G/A snv 0.15 4
rs7107356 1.000 0.040 11 47654618 downstream gene variant A/G snv 0.45 4
rs754593
MAPT
1.000 0.040 17 45977330 non coding transcript exon variant G/A snv 0.52 4
rs8089865
DCC
1.000 0.040 18 53431552 intron variant G/A;C snv 4
rs878567
HTR1A
0.882 0.040 5 63960164 intron variant A/C;G snv 4
rs10965780 1.000 0.040 9 23341717 intron variant C/G;T snv 3
rs111365677 0.925 0.040 1 99463578 upstream gene variant T/C snv 2.3E-03 3
rs112106319
TNC ; DELEC1
0.925 0.040 9 115094539 intron variant A/T snv 2.8E-03 3
rs112538845 0.925 0.040 4 184084475 downstream gene variant C/T snv 1.7E-02 3
rs113378111 1.000 0.040 2 9788024 intergenic variant G/A snv 2.8E-02 3
rs114465512
IGLV10-54
1.000 0.040 22 22047895 intron variant C/T snv 4.7E-03 3
rs117198528
LOC105372112
1.000 0.040 18 49694188 intergenic variant T/G snv 1.0E-02 3
rs11924809
DGKG
0.925 0.040 3 186353656 intron variant G/A snv 5.3E-02 3
rs12963463
TCF4
1.000 0.040 18 55431862 intron variant C/G;T snv 3
rs138472420
BICRA
1.000 0.040 19 47657765 intron variant G/A snv 3.3E-03 3
rs141746753 1.000 0.040 8 56934154 intergenic variant C/T snv 3.1E-03 3
rs142484554
SPSB4
0.925 0.040 3 141059454 intron variant GAG/- delins 0.11 3